BEUDAMED
    9 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    P.F.C. 28MM HEAD +5 MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code KWY·July 15, 2011

    P.F.C. LINR 48-52/10 DEG-28MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JDI·July 15, 2011

    P.F.C. TOTAL HIP SYSTEM FEMORAL HEAD COMPONENT

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON PROFESSIONAL, INC.·Product code KWY·March 25, 1997

    P.F.C. BIPOLAR HEAD LINER COMPONENT

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON PROFESSIONAL, INC.·Product code KWB·March 25, 1997

    STELLARIS MICROSURGICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQC·April 18, 2014

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·December 3, 2012

    SHILEY DISPOSABLE CANNULA LOW PRESSURE

    FDA Adverse Event
    Malfunction ·COVIDIEN/ FORMERLY TYCO HEALTHCARE·Product code JOH·September 8, 2010

    PFC TOTAL HIP SYSTEM- BIPOLAR LINER

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON PROFESSIONALS, INC.·Product code KWB·August 11, 1997

    PFC TOTAL HIP SYSTEM- FEMORAL HIP HEAD

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON PROFESSIONALS, INC.·Product code KWY·August 11, 1997